Martin Chevarin

13PUBLICATIONS
74CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeonatologyRecordkeeping informatics
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Publications (13)

|Oct 23, 2025
PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France.

Camille Level, Christel Thauvin-Robinet, Christine Binquet

|Oct 18, 2023
Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples.

Robin Wijngaard, German Demidov, Luke O'Gorman

|Nov 30, 2022
A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort.

Philippine Garret, Martin Chevarin, Antonio Vitobello

|Aug 26, 2022
Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study.

Eloïse Bailly, Stéphane Valot, Anne Vincent

|May 16, 2022
Same performance of exome sequencing before and after fetal autopsy for congenital abnormalities: toward a paradigm shift in prenatal diagnosis?

Nicolas Bourgon, Aurore Garde, Ange-Line Bruel

|Feb 20, 2020
Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20.

Aurélien Juven, Sophie Nambot, Amélie Piton

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Frequent Collaborators

5 joint publications

Paul Kuentz

5 joint publications

Antonio Vitobello

4 joint publications

Julien Thevenon

4 joint publications

Anne-Sophie Denommé-Pichon